A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687171



Internal ID110837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41560958..41560958hg38UCSC Ensembl
chr13:42135094..42135094hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381618
hg191618
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548424
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687171
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.470049


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